PMC Links for Nucleotide (Select 1677531434) - PMC

Select item 62901011.

PHF6 and DNMT3A mutations are enriched in distinct subgroups of mixed phenotype acute leukemia with T-lineage differentiation

Wenbin Xiao, Maheetha Bharadwaj, Max Levine, Noushin Farnhoud, Friederike Pastore, Bartlomiej M. Getta, Anne Hultquist, Christopher Famulare, Juan S. Medina, Minal A. Patel, Qi Gao, Natasha Lewis, Janine Pichardo, Jeeyeon Baik, Brian Shaffer, Sergio Giralt, Raajit Rampal, Sean Devlin, Robert Cimera, Yanming Zhang, Maria E. Arcila, Elli Papaemmanuil, Ross L. Levine, Mikhail Roshal

Blood Adv. 2018 Dec 11; 2(23): 3526–3539. Published online 2018 Dec 10. doi: 10.1182/bloodadvances.2018023531

Correction in:: Blood Adv. 2019 Apr 9; 3(7): 956.

PMCID:: PMC6290101

Abstract Article PDF–1.4M

Select item 57743602.

Coexistence of EZH2, NOTCH1, IL7R, and PHF6 Mutations in Adult T-cell Acute Lymphoblastic Leukemia

Xilian Zhou, Yan Gu, Qi Han, Mario Soliman, Chunhua Song, Zheng Ge

Turk J Haematol. 2017 Dec; 34(4): 366–368. Published online 2017 Dec 1. doi: 10.4274/tjh.2017.0194

PMCID:: PMC5774360

Article PDF–439K

Select item 51028433.

Pathogenesis of Börjeson-Forssman-Lehmann Syndrome: Insights from PHF6 Function

Arezu Jahani-Asl, Cheng Cheng, Chi Zhang, Azad Bonni

Neurobiol Dis. Author manuscript; available in PMC 2017 Dec 1.

Published in final edited form as: Neurobiol Dis. 2016 Dec; 96: 227–235. Published online 2016 Sep 12. doi: 10.1016/j.nbd.2016.09.011

PMCID:: PMC5102843

Abstract Article PDF–529K

Select item 17354154.

Novel PHF6 mutation p.D333del causes Börjeson-Forssman-Lehmann syndrome

A Baumstark, K Lower, A Sinkus, I Andriuskeviciute, L Jurkeniene, J Gecz, W Just

J Med Genet. 2003 Apr; 40(4): e50. doi: 10.1136/jmg.40.4.e50

PMCID:: PMC1735415

Summary PDF–220K

Select item 66942315.

Genetic variants and clinical significance of pediatric acute lymphoblastic leukemia

Hong-Hong Zhang, Hong-Sheng Wang, Xiao-Wen Qian, Cui-Qing Fan, Jun Li, Hui Miao, Xiao-Hua Zhu, Yi Yu, Jian-Hua Meng, Ping Cao, Jun Le, Jun-Ye Jiang, Wen-Jing Jiang, Ping Wang, Xiao-Wen Zhai

Ann Transl Med. 2019 Jul; 7(14): 296. doi: 10.21037/atm.2019.04.80

PMCID:: PMC6694231

Abstract Article PDF–1.1M

Select item 66100366.

Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum

Alain Sarasin, Samuel Quentin, Nathalie Droin, Mourad Sahbatou, Véronique Saada, Nathalie Auger, Yannick Boursin, Philippe Dessen, Anna Raimbault, Vahid Asnafi, Jean-Luc Schmutz, Alain Taïeb, Carlos F. M. Menck, Filippo Rosselli, Laurianne Drieu La Rochelle, Caroline Robert, Flore Sicre de Fontbrune, Marie Sébert, Thierry Leblanc, Patricia Kannouche, Stéphane De Botton, Eric Solary, Jean Soulier

Blood. 2019 Jun 20; 133(25): 2718–2724. Prepublished online 2019 Mar 26. doi: 10.1182/blood-2019-01-895698

PMCID:: PMC6610036

Abstract Article

Select item 65823137.

Exosomal hsa-miR199a-3p Promotes Proliferation and Migration in Neuroblastoma

Jing Ma, Min Xu, Minzhi Yin, Jie Hong, Haoyan Chen, Yijin Gao, Chenjie Xie, Nan Shen, Song Gu, Xi Mo

Front Oncol. 2019; 9: 459. Published online 2019 Jun 12. doi: 10.3389/fonc.2019.00459

PMCID:: PMC6582313

Abstract Article PDF–1.7M

Select item 57071858.

Detection of Mutations in Myeloid Malignancies through Paired-Sample Analysis of Microdroplet-PCR Deep Sequencing Data

Donavan T. Cheng, Janice Cheng, Talia N. Mitchell, Aijazuddin Syed, Ahmet Zehir, Nana Yaa T. Mensah, Alifya Oultache, Khedoudja Nafa, Ross L. Levine, Maria E. Arcila, Michael F. Berger, Cyrus V. Hedvat

J Mol Diagn. 2014 Sep; 16(5): 504–518. doi: 10.1016/j.jmoldx.2014.05.006

PMCID:: PMC5707185

Abstract Article PDF–1.3M

Select item 43376149.

miR-128 regulates neuronal migration, outgrowth and intrinsic excitability via the intellectual disability gene Phf6

Eleonora Franzoni, Sam A Booker, Srinivas Parthasarathy, Frederick Rehfeld, Sabine Grosser, Swathi Srivatsa, Heiko R Fuchs, Victor Tarabykin, Imre Vida, F Gregory Wulczyn

eLife. 2015; 4: e04263. Published online 2015 Jan 3. doi: 10.7554/eLife.04263

PMCID:: PMC4337614

Abstract Article PDF–4.5M

Select item 315556710.

Transcriptional Profiling of Human Liver Identifies Sex-Biased Genes Associated with Polygenic Dyslipidemia and Coronary Artery Disease

Yijing Zhang, Kathrin Klein, Aarathi Sugathan, Najlla Nassery, Alan Dombkowski, Ulrich M. Zanger, David J. Waxman

PLoS One. 2011; 6(8): e23506. Published online 2011 Aug 12. doi: 10.1371/journal.pone.0023506

PMCID:: PMC3155567

Abstract Article PDF–707K

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